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Sanofi’s Altuviiio Set To Reenergize Factor VIII Space

 
• By Jessica Merrill

The once-weekly Factor VIII replacement therapy for hemophilia A, newly approved by the US FDA, appears well positioned to compete with Roche’s blockbuster Hemlibra.

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The US Food and Drug Administration approval of Sanofi’s next-generation Factor VIII replacement therapy Altuviiio (efanesoctocog alfa) for hemophilia A appears to give the company a sound foothold to compete in the commercial market against Roche Holding AG’s monoclonal antibody Hemlibra (emicizumab).

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